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新型聚砜透析器的性能和血液相容性:一项随机对照试验。

Performance and Hemocompatibility of a Novel Polysulfone Dialyzer: A Randomized Controlled Trial.

机构信息

Clinic for Hypertension, Kidney and Metabolic Diseases Hannover, Hannover, Germany.

Global Research and Development, Fresenius Medical Care, St. Wendel, Germany.

出版信息

Kidney360. 2021 Apr 7;2(6):937-947. doi: 10.34067/KID.0000302021. eCollection 2021 Jun 24.

Abstract

BACKGROUND

High-flux dialyzers effectively remove uremic toxins, are hemocompatible to minimize intradialytic humoral and cellular stimulation, and have long-term effects on patient outcomes. A new dialyzer with a modified membrane surface has been tested for performance and hemocompatibility.

METHODS

This multicenter, prospective, randomized, crossover study involved the application of the new polysulfone-based FX CorAL 600 (Fresenius Medical Care, Bad Homburg, Germany), the polyarylethersulfone-based Polyflux 170H (Baxter Healthcare Corporation, Deerfield, IL), and the cellulose triacetate-based SureFlux 17UX (Nipro Medical Europe, Mechelen, Belgium), for 1 week each, to assess the noninferiority of the FX CorAL 600's removal rate of 2-microglobulin. Performance was assessed by removal rate and clearance of small- and medium-sized molecules. Hemocompatibility was assessed through markers of complement, cell activation, contact activation, and coagulation.

RESULTS

Of 70 patients, 58 composed the intention-to-treat population. The FX CorAL 600's removal rate of 2-microglobulin was noninferior to both comparators (<0.001 versus SureFlux 17UX; =0.0006 versus Polyflux 170H), and superior to the SureFlux 17UX. The activation of C3a and C5a with FX CorAL 600 was significantly lower 15 minutes after treatment start than with SureFlux 17UX. The activation of sC5b-9 with FX CorAL 600 was significantly lower over the whole treatment than with SureFlux 17UX, and lower after 60 minutes than with the Polyflux 170H. The treatments with FX CorAL 600 were well tolerated.

CONCLUSIONS

FX CorAL 600 efficiently removed small- and medium-sized molecules, showed a favorable hemocompatibility profile, and was associated with a low frequency of adverse events in this study, with a limited patient number and follow-up time. Further studies, with longer observation times, are warranted to provide further evidence supporting the use of the new dialyzer in a wide range of therapeutic options, and for long-term treatment of patients on hemodialysis, to minimize the potential effects on inflammatory processes.

摘要

背景

高通量透析器能有效清除尿毒症毒素,血液相容性好,可最大限度减少透析过程中的体液和细胞刺激,对患者预后有长期影响。一种新型改良膜表面透析器已进行性能和血液相容性测试。

方法

这是一项多中心、前瞻性、随机、交叉研究,应用新型聚砜基 FX CorAL 600(费森尤斯医疗保健公司,德国巴特洪堡)、聚芳醚砜基 Polyflux 170H(百特医疗保健公司,伊利诺伊州迪尔菲尔德)和三醋酸纤维素基 SureFlux 17UX(日机装株式会社,比利时梅赫伦),每周各使用 1 周,以评估 FX CorAL 600 对β2-微球蛋白清除率的非劣效性。通过小分子和中分子的清除率和清除率来评估性能。通过补体、细胞激活、接触激活和凝血的标志物评估血液相容性。

结果

在 70 名患者中,58 名患者构成意向治疗人群。FX CorAL 600 对β2-微球蛋白的清除率非劣于两种对照剂(<0.001 与 SureFlux 17UX;=0.0006 与 Polyflux 170H),且优于 SureFlux 17UX。FX CorAL 600 治疗开始后 15 分钟,C3a 和 C5a 的激活明显低于 SureFlux 17UX。FX CorAL 600 治疗期间 sC5b-9 的激活明显低于 SureFlux 17UX,60 分钟后低于 Polyflux 170H。FX CorAL 600 治疗耐受性良好。

结论

FX CorAL 600 能有效清除小分子和中分子,血液相容性良好,在这项研究中,与 SureFlux 17UX 相比,不良事件发生率低,患者数量和随访时间有限。需要进一步的研究,观察时间更长,以提供更多证据支持新型透析器在广泛的治疗选择中的应用,并为长期血液透析患者提供治疗,以最大限度地减少对炎症过程的潜在影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3096/8791382/e1eb3f760515/KID.0000302021absf1.jpg

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